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169452-08-8

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169452-08-8 Usage

General Description

1-(4-Fluoro-benzyl)-pyrrolidin-3-ylamine dihydrochloride is a chemical compound that belongs to the class of pyrrolidines. It is a dihydrochloride salt form of 1-(4-fluoro-benzyl)-pyrrolidin-3-ylamine, which acts as a selective antagonist for the nociceptin/orphanin FQ (NOP) receptor. This chemical compound is commonly used in research studies to understand its potential in pain management and treatment of other neurological disorders. It is an important tool in the exploration of the NOP receptor and its role in the human body. Additionally, its dihydrochloride form makes it more stable and suitable for laboratory use.

Check Digit Verification of cas no

The CAS Registry Mumber 169452-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,4,5 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 169452-08:
(8*1)+(7*6)+(6*9)+(5*4)+(4*5)+(3*2)+(2*0)+(1*8)=158
158 % 10 = 8
So 169452-08-8 is a valid CAS Registry Number.

169452-08-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-fluorophenyl)methyl]pyrrolidin-3-amine,dihydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:169452-08-8 SDS

169452-08-8Downstream Products

169452-08-8Relevant articles and documents

Triazinone compound and T-type calcium channel inhibitor

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Page/Page column 87; 88, (2016/08/29)

There is provided a novel triazinone compound that has an excellent T-type voltage-dependent calcium channel inhibitory activity and is specifically useful for treatment of pain. A compound of Formula (I), a tautomer of the compound, a pharmaceutically acceptable salt thereof, or a solvate thereof: where each substituent is defined in detail in the description or claims, for example R1 is H or C1-6 alkoxy, etc., each of L1 and L2 is independently a single bond or NR2, etc., L3 is C1-6 alkylene, etc., A is C6-14 aryl or 5 to 10-membered heteroaryl which is optionally substituted, etc., B is C3-11 cycloalkylene, etc., D is C6-14 aryl or 5 to 10-membered heteroaryl which is optionally substituted, etc.

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